2lgi | pdb_00002lgi

Atomic Resolution Protein Structures using NMR Chemical Shift Tensors

spinqualitylabelsall models 2lgi, 10 NMR models Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 2lgi is a 1 chain structure with sequence from Strsg. Full experimental information is available from OCA. For a guided tour on the structure components use FirstGlance. Related: 2kwd, 2kq4, 2kop, 2jsv, 2qmt, 2ju6, 2plp, 2gi9, 1pga, 1pgb, 1gb1, 2gb1 Gene: spg (STRSG) Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum Function [SPG1_STRSG] Binds to the constant Fc region of IgG with high affinity. Publication Abstract from PubMed NMR chemical shift tensors (CSTs) in proteins, as well as their orientations, represent an important new restraint class for protein structure refinement and determination. Here, we present the first determination of both CST magnitudes and orientations for (13)Calpha and (15)N (peptide backbone) groups in a protein, the beta1 IgG binding domain of protein G from Streptococcus spp., GB1. Site-specific (13)Calpha and (15)N CSTs were measured using synchronously evolved recoupling experiments in which (13)C and (15)N tensors were projected onto the (1)H-(13)C and (1)H-(15)N vectors, respectively, and onto the (15)N-(13)C vector in the case of (13)Calpha. The orientations of the (13)Calpha CSTs to the (1)H-(13)C and (13)C-(15)N vectors agreed well with the results of ab initio calculations, with an rmsd of approximately 8 degrees . In addition, the measured (15)N tensors exhibited larger reduced anisotropies in alpha-helical versus beta-sheet regions, with very limited variation (18 +/- 4 degrees ) in the orientation of the z-axis of the (15)N CST with respect to the (1)H-(15)N vector. Incorporation of the (13)Calpha CST restraints into structure calculations, in combination with isotropic chemical shifts, transferred echo double resonance (13)C-(15)N distances and vector angle restraints, improved the backbone rmsd to 0.16 A (PDB ID code 2LGI) and is consistent with existing X-ray structures (0.51 A agreement with PDB ID code 2QMT). These results demonstrate that chemical shift tensors have considerable utility in protein structure refinement, with the best structures comparable to 1.0-A crystal structures, based upon empirical metrics such as Ramachandran geometries and chi(1)/chi(2) distributions, providing solid-state NMR with a powerful tool for de novo structure determination. Ultrahigh resolution protein structures using NMR chemical shift tensors.,Wylie BJ, Sperling LJ, Nieuwkoop AJ, Franks WT, Oldfield E, Rienstra CM Proc Natl Acad Sci U S A. 2011 Oct 11;108(41):16974-9. Epub 2011 Oct 3. PMID:21969532 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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